Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12655443 1.000 0.080 5 142088291 regulatory region variant C/A;T snv 2
rs3813308 1.000 0.080 5 119355086 5 prime UTR variant C/G snv 0.37 2
rs4910165 11 10652497 intron variant C/G snv 0.78 2
rs10788639 10 80473469 intron variant C/G snv 0.64 1
rs72938315 2 203256340 intron variant C/G snv 0.11 1
rs4129267 0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs9979383 0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs1950897 0.925 0.160 14 68293424 intron variant C/G;T snv 3
rs2811387 3 128296335 intron variant C/G;T snv 3
rs10965935 9 23581213 intron variant C/G;T snv 0.38 1
rs1779774 6 63500578 intergenic variant C/G;T snv 1
rs2949669 1 167448647 intron variant C/G;T snv 1
rs41283642 9 99153605 3 prime UTR variant C/G;T snv 1
rs802731 6 127958284 intergenic variant C/G;T snv 1
rs3785356 0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs11071559 0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs12123821 0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 4
rs3122929 0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs11495981 1.000 0.120 7 28137682 intron variant C/T snv 0.29 2
rs115008099 1.000 0.080 5 132656189 intron variant C/T snv 0.15 2
rs7130870 1.000 0.080 11 36322652 intron variant C/T snv 0.27 2
rs111782388
ITK
5 157202838 intron variant C/T snv 6.3E-02 1
rs11255938 10 8808772 intergenic variant C/T snv 0.34 1
rs117552144 19 3136093 5 prime UTR variant C/T snv 3.8E-02 1
rs61957178 13 73421057 intron variant C/T snv 0.19 1